| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:47758852-47759237 | Common:3; Rare:80 | ||||
| chr12:47797470-47797520 | Rare:9 | ||||
| chr12:47904977-47905128 | Common:1; Rare:43; Clinvar:1 | ||||
| chr12:48105818-48106158 | Common:2; Rare:99 | ||||
| chr12:48106240-48106388 | Rare:42 | ||||
| chr12:48141312-48141616 | Common:1; Rare:48; Clinvar (benign):2 | ||||
| chr12:48350786-48350942 | Rare:59 | ||||
| chr12:48716639-48717046 | Common:4; Rare:123 | ||||
| chr12:48774188-48774456 | Common:1; Rare:57 | ||||
| chr12:48774541-48774740 | Rare:56 | ||||
| chr12:48814383-48814502 | Common:1; Rare:23 | ||||
| chr12:48814664-48814862 | Rare:34 | ||||
| chr12:48815451-48815636 | Common:1; Rare:42 | ||||
| chr12:48839843-48840096 | Rare:65 | ||||
| chr12:48852085-48852431 | Common:2; Rare:96 |